PRAVASTATIN SODIUM
- Product NDC
- 55801-144
- 11-digit product format
- 558010144
- Labeler code
- 55801
- Product ID
- 55801-144_6e0a1a56-f6dd-4c55-9b48-df317f5bfff6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PRAVASTATIN SODIUM
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- APPCO PHARMA LLC
- Application
- ANDA209869
- Marketing category
- ANDA
- Marketing start
- 2018-04-13
- Marketing end
- 0000-00-00
- Substance
- PRAVASTATIN SODIUM
- Active strength
- 80 mg/1
- Pharmacologic classes
- HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record